01 1Divi’s Laboratories
02 1M/s. Global Calcium Pvt. Ltd.,
01 1Phenprocoumon
02 1Phenprocoumon (IH)
01 1WC-0031
02 1WC-0104
01 2India
Date of Issue : 2022-06-16
Valid Till : 2025-06-16
Written Confirmation Number : WC-0031
Address of the Firm : Unit-Lingojigudem (V) Choutuppal (M) Nalgonda District Talangana State India
Date of Issue : 2022-06-08
Valid Till : 2025-07-07
Written Confirmation Number : WC-0104
Address of the Firm : #125 & 126, Sipcot Industrial Complex, Hosur-635 126, Tamilnadu
49
PharmaCompass offers a list of Phenprocoumon API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Phenprocoumon manufacturer or Phenprocoumon supplier for your needs.
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A Falithrom manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Falithrom, including repackagers and relabelers. The FDA regulates Falithrom manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Falithrom API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Falithrom supplier is an individual or a company that provides Falithrom active pharmaceutical ingredient (API) or Falithrom finished formulations upon request. The Falithrom suppliers may include Falithrom API manufacturers, exporters, distributors and traders.
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A Falithrom written confirmation (Falithrom WC) is an official document issued by a regulatory agency to a Falithrom manufacturer, verifying that the manufacturing facility of a Falithrom active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Falithrom APIs or Falithrom finished pharmaceutical products to another nation, regulatory agencies frequently require a Falithrom WC (written confirmation) as part of the regulatory process.
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